CA1193374A - Polybutadiene rubber compositions - Google Patents
Polybutadiene rubber compositionsInfo
- Publication number
- CA1193374A CA1193374A CA000408228A CA408228A CA1193374A CA 1193374 A CA1193374 A CA 1193374A CA 000408228 A CA000408228 A CA 000408228A CA 408228 A CA408228 A CA 408228A CA 1193374 A CA1193374 A CA 1193374A
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- rubber composition
- polybutadiene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/16—Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/26—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment
- C08L23/28—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or compounds containing halogen
- C08L23/283—Halogenated homo- or copolymers of iso-olefins
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
- C08L23/22—Copolymers of isobutene; Butyl rubber ; Homo- or copolymers of other iso-olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/02—Copolymers with acrylonitrile
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
- C08L9/06—Copolymers with styrene
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Abstract of the Disclosure A rubber composition having excellent fracture properties and cut growth resistance is disclosed, which consists of 10-95 parts by weight of polybutadiene having a content of cis-1,4 bond of at least 70% and an average chain length of 1,4 sequence of 110-450 and 90-5 parts by weight of at least one diene rubber.
Description
~33~7~
This inventio-n relates to rubber compositions and curable rubber compositions each including polybutadiene with a particular average chain leng-th of 1,4-sequence and having excellent fracture properties and cut grow-th resist-ance.
Heretofore, high cis-type polybutadiene rubber compositions have been applied for various members in tire indus-try such as sidewall rubber, tread rubber, rubber chafer, base rubber and the like because they are charac-terized by having an excellent flex resistance and a low energy loss. However, these conventional polybutadiene rubbers are small in the fracture properties and poor in the CUt growth resistance as compared with the other diene rubbers, so that they are naturally restricted in use and also the blending ratio -to the other rubber is restrained within a rel.atively l.ow range. As a result, satisfactory polybutacliene rubber compositions are not yet obtained up to now.
The inventors have made various studies in order to improve the above menti.oned drawback of the prior art and found that polybutadiene having a particular range of average chain length of l,4-sequence provides a rubber composition having excellent fracture properties and cut growth resistance, and as a result the invention has been accomplished.
According to the invention, there is the provision of a rubber composition having excellent fracture properties and cut growth resistance, consisting of 10 to 95 parts by weight of polybutadiene having a content of cis 1,4 bond of at least 70% and an average chain leng~h of 1,4-sequence
This inventio-n relates to rubber compositions and curable rubber compositions each including polybutadiene with a particular average chain leng-th of 1,4-sequence and having excellent fracture properties and cut grow-th resist-ance.
Heretofore, high cis-type polybutadiene rubber compositions have been applied for various members in tire indus-try such as sidewall rubber, tread rubber, rubber chafer, base rubber and the like because they are charac-terized by having an excellent flex resistance and a low energy loss. However, these conventional polybutadiene rubbers are small in the fracture properties and poor in the CUt growth resistance as compared with the other diene rubbers, so that they are naturally restricted in use and also the blending ratio -to the other rubber is restrained within a rel.atively l.ow range. As a result, satisfactory polybutacliene rubber compositions are not yet obtained up to now.
The inventors have made various studies in order to improve the above menti.oned drawback of the prior art and found that polybutadiene having a particular range of average chain length of l,4-sequence provides a rubber composition having excellent fracture properties and cut growth resistance, and as a result the invention has been accomplished.
According to the invention, there is the provision of a rubber composition having excellent fracture properties and cut growth resistance, consisting of 10 to 95 parts by weight of polybutadiene having a content of cis 1,4 bond of at least 70% and an average chain leng~h of 1,4-sequence
- 2 -. .
r; ~
of 110 to 450 and 90 to 5 par-ts by weight of at least one diene rubber.
The invention will be described in detail below.
The avera~e chaîn length of 1,4-sequence defined in the invention is measured as follows. That is, the polybutadiene accordin~ to the invention is completely hyclrogena~ed with p-toluenesulfonyl hydrazide according to a method disclosed in Makromol. Chem., 163, l (1973) to obtain a hydrogenation product to be tested. In this case, the completion of hydrogenation is confirmed by means of Hl-NM~. Then, the hydrogena~ion product or hydrogenated polybutadiene is measured with respect to average chain length of 1,4-sequence under the :Eollowing conditions using a nuclear magnetic resonance (NMR) apparatus of F~-lO0 Model made by Nippon Denki Kabushiki Kaisha:
Concentration of test sample : 300 mg/2 ml 1,2,4-trichlorobenzene with perdeuterobenzene, use of lO mm~ probe for l~C-NMR, Carrier frequency : 25.05 MHz, internal lock system, Flip angle : 45, Pulse width : 6 ~sec, Ac~uisition time : 5.0 sec, Spectrum sweep width : 2 KHz, Measuring tempera~ure : 125C, Internal reference : HMDS, Number of scan : llOxlO0 to l90xlO0 times.
~ 33~
Fu:rther, a-verage chain lengLhs of 1,2-sequence and 1,4-sequence are analyzed by the following equa-tions according to a method disclosed in J. Polymer Sci., Polymer Physics Edition, 13, 1975 (1975):
Average chain length of 1~2-sequence = 5I + 6 8 Average chain length of 1,4-sequence = ~ 8I 104I 11 , wherein each of I5, 1~, I8, Ig~ Ilo and I11 is an intensity o peak area at each of 37.2, 34.8, 34.0, 31.0~ 30.5 and 30.0 ppm. The assignment of the analytical results is shown in the following Table 1.
~ ~, ~3~
Table l Chemical Equation ~Ll Assignment shi-F-t (ppm) L2 r Il k r~2 (r~l)N01(13rl~ /V\(\~ V\/V 40-4 I2 = kNolo /V\/yVVVV 40 . 3 ~3 2k ?r~l NOl(l)rlO /V\~ (VVV 39 7 = kNollo /VV\~VVV\ 39.O
Is = 2k ~0 NOl(l)rl /V~yy\/v 37.2 r~O Ol ( l ) rlO /Vyyyv\ 34 . 8 r I7 21c ~O Nol(l)rl /\/~y\~/\ 34 5 I8 = 21cNolo /V\~/\ 34. O
19 = kNlo1 /yVVy\ 31. O
10 ~_o l O ( O ) sOl y\~v\~Vy\ 30 . 5 Ill k ~0 (4s~3 )Nlo ( o ~ sO] yv'~/vyv I12 = 2kNolo /V\~y\~v 27 . 3 I15 = kNolo /VvyVv 26. 7 Il6 = kNolo VVV\~VV ll.1 V~
~3 Ir ~
Note) I1, I2, ..., I16 shows an intensity of peak area at respective chemical shift, and r is 1,2-sequence, and s is 1,4-sequence.
~2 : found value of chemical shift.
Further J a heat vf fusion of the hydrogenation product of polybu-tadiene according to the invention is equivalent to the average chain length of 1,4-sequence, but it is preferable within a range of 42-135 cal/g.
The heat of fusion is measured from a fusion peak area obtained by placing abouL 10 mg of the hydrogenated poly-butadiene on an alwminum dish and raising temperature at a rate of 20C/min in a differential scanning calorimeter ~made by Rigaku Corp.). When the heat of fusion is less than 42 cal/g, the average chain length of 1,4-sequence does not rea$h into 110, while when the heat of fus:ion exceeds 135 cal/g, the average chain length of 1,4-sequence also exceeds 450.
The content of cis-1,4 bond is measured by means of the NMR apparatus.
The polybutadiene according to the invention having a particular average chain length of l,4-sequence can be produced, for example, by polymerizing butadiene in the presence of a catalyst consisting of a combination of a compound of lan~hanum series rare ear-th element (herein-after referred to as Ln compound), an organoaluminum compound and Lewis acid a-nd/or Lewis base.
As the Ln compound, there are used halides, carboxylates, alcoholates 9 thioalcvholates, amides and -the 37i~
like of metals having an atomic number of 57-71.
As the organoaluminum compound, ~here are used ones having a general formula of AlRlR2R3, wherein Rl, R2 and R3 are the same or differen~ and represent a hydrogen atom or a hydrocarbon residue havillg a carbon atom of 1-8, respectively.
As the Lewis acid, there are used aluminum halides having a general formula of AlXnR3 n~ wherein X is a halogen atom, R is a hydrocarbon residue and n is 1, 1.5, 2 or 3, or the other metal halides.
The Lewis base is used for solubilizing the Ln compound in an organic solvent. For instance, acetylacetone, ketone and the like are preferably used.
The mole ratio of butadiene to Ln compound is 5x10~-5x106, preferably 103-105. The mole ratio of AlR1R2R3 to Ln compound is 5-500, preferably 10-300. The mole ratio of halide in Lewis acid to Ln compound is 1-10, preferably 1~5-S. The mole ratio of I.ewis base to Ln compound is noL less than O.S, preferably 1-20.
According to the invention, the average chain length o~ 1,4-sequence is 110-450, preferably 130-300.
When the average chain length is less than 110, there is no effect for the improvement of cut growth resistance, while when the average chain length exceeds 450, the resulting polybutadiene is apt to be fatigued. For instance, when the polybu~adiene is subjected to repetitive stretching in a given direction over a long ~ime, a tear s~rength after a cut is formed in parallel with the stretching direction considerably reduces.
The polybutadiene according to the inventio-n has a content of cis-1,4 bond of a~ leas-t 70%, preferably no~
less ~han 90/O~ more particwlar:Ly 90-98%. When the content o-f cis-1,4 bond is less than 70%, the property of low energy loss disappears.
As the diene rubber to 'he used in the inven~ion, mention may be made of natural rubber, polyisoprene rubber, styrene~'butadiene copolymer rub'ber, acrylonitrile-butadiene copolymer rubber, ethylene-propylene-diene terpolymer rubber, isobutylene-isoprene copolymer rubber, halogenated-(isobutylene-isoprene copolymer) rubber and the like.
In the rubber composition according to the invention, the blending ratio of polybutadiene to diene ru'bber is 10-95 parts by weight to 90-5 parts by weight, preferably 30-95 parts by ~eight to 70-5 par~s by weight.
When the amount of polybutadiene rubber is less than 10 parts by weight, the blencling effect is not obtained, while when the amount of polybutadiene exceeds 95 parts by weight, the roll workabi:Lity becomes impractically poor.
To 100 parts by weight of the rubber composition according to the invention may be added 20-120 parts by weight of an inorganic filler and 0 5-10 parts by weight of a vulcanizing agent to form a curable rubber composition.
As the inorganic filler, use may be made of silicic anhydride, calcium carbonate, magnesium carbonate, talc, iron sulfide, iron oxide, bentonite, zinc white~
diatomaceous earth, china cla~, clay, alumina, titanium oxide, carbon black and the like When the amount of inorganic filler i5 less than 20 parts by weight, sufficient rein~orcing effec-t is not o'btained, while when -the amount of inorgan:ic filler exceeds 120 parts by weight, the ~33~'~
workability considerably lowers.
As the vulcaniæ:ing agent, mention ma.y be made of sulfur, p-quinonedioxime, p,p'-dibenzoylquinonedioxime, 4,4'-dithiodimorpholine, poly-p-dinitrobenzene5 ammoni.um benzoate, alkylphenol dis-ulficle and the like. Further, such a vulcanizing agent may be used together with peroxide.
~hen the amount of vulcanizing agent is ]ess than 0.5 part by weight, sufficient vulcanizing ef:Eect cannot be expected, while when the amount of vulcanizing agent exceeds 10 par-ts by wei.ght, ~.he resulting vulcani.zate is too hard and the elasticity of rubber in itself cannot be expected.
To the ruhber composition according to the invention may be added additives usually used in rubber industry such as softener, process oil, pigment, vulcaniza-lS tion accelerator and the lilce in addîtion to the above mentioned additives. Carbon black is preferable to have an iodine adsorption number of 30-150 mg/g and a dibutyl phthalate adsorption number of 45-140 cm3/100 g.
The mixing of i.ngredients forming the rubber composition according to the invention is per.Eormed by means of roll mill, Banbury mixer, extruder or the like in the usual manner. In this case, it is favorable to uniformly mix these ingredients at a state near the orcler of molecule.
The rubber compositions accord.ing to the invention are excellent in the fracture properties and cut growth resistance, so that they can wi.dely be used as industrial goods such as tires, conveyor belts, hoses and the like.
The following examples are given in illustration o-f the invention and are not intendecl as limitations thereof.
g 7'.~
Examples 1-4 Into a sufficiently dried glass autoclave of 5 Q
capacity was charged 2.5 kg of cyclohexane under a nitrogen atmosphere and further 0. 5 kg of butadiene, and then the temperature of the autoclave was raised to 60C. A reaction product of 138.9 mM of triethylaluminum, 2.31 mM of diethyl-aluminum bromide, 0.926 mM of neodymium octenoate and 1.85 mM of acetylacetone was previously aged as a catalyst in another vessel in the presence of 0.1 g of butadiene and then charged into the autoclave a~ once to star~
polymerization. After two hours of polymerization, -the degree of conversion reached to 100%. At this time, 5 ml of methanol solution containi.ng 2,6-di-tert-butyl cresol as an antioxidant was pourecl into the autoclave to stop polymerization reaction. The resulting polymerization product was subjected to st.eam stripping in the usual manner and dried on a hot roll ot 110C to obtain a poly-butadi.ene, which is called as Sample No. 4 hereinafter.
Ln the following Table 2 are shown measured values of average chain length of 1,4-sequence, micro-structure and calorimetric analysis of various polybutadiene samples.
In Table 2, Sample No. 1 is a polybutadiene rubber made by Anic Corp. using an uranium catalyst.
Sample No. 2 is obtained by dissolving each of Sample Nos. 1 and 4 in n-hexane and blending them at a blending ratio of Sample No. 1 to Sample No. 4 of 1:4. Sample No. 3 is obLained by blending Sample No. 1 and Sample No. 4 at a blending ratio of 4:6 in the same manner as described on Sample No. 2. Sample No. 6 is a polybutadiene rubber 37'~
made by Japan Synthetic Rubber Kabushiki Kaisha (trade mark ~R01). Sample No. 5 is obtained by dissolving each of Sample Nos. 4 and 6 in n-hexane and blending ~hem at a blending ratio of Sample No. 4 to Sample No. 6 of 1:4. Sample No, 7 is a polybu-~adiene rubber made by Ube Kosan Kabushiki Kaisha (trade mark UBEPOL 150). Sample No. 8 is a polybutadiene rubber made by Japan Synthetic Rubber Kabushiki Kaisha (trade mark BR02). Sample No. 9 is a polybutadiene rubber made by Philips Chemical Company (trade mark CIS-4 1203)... Sample No. 10 is a polybutadiene rubber made by Asahi Kasei Kabushiki Kaisha (trade mark DIENE 35 NF).
Table 2 ].5 \ A~erage chain Microstructure Calorimetric \ Items lengths of analysis \ 1,4- and 1,2-Poly- \ sequences cis;1,4 tla45 1j2 fusatOnf Tm butadiene \ 1,4 1,2 (%) (cal/g) Sample No. 1 523 1.0 97.4 1.2 1.4156 130 Sample No. 2 441 1.0 97.0 1.5 1.5130 129 Sample No. 3 300 1.0 96.2 2.0 1.895 129 Sample No~ 4 152 1.0 95.3 2.5 2.251 129 Samp].e No. 5 113 1.0 95.0 2.8 2.2 43 124 Sample No. 6 10~ 1.0 94.9 2.9 2.243 123 Sample No. 7 70 1.0 9~5 2.6 2.939 120 Sample No. 8 20 1.0 94.2 2.5 3.332 112 Sample No. 9 18 1.0 88.8 4.7 5.229 1~0 Sample No. 10 14 1.1 32.7 53.2 14.024 93 0 Note) Heat o fusion (cal/g) was measured from the hydro~enated sample as previously mentioned.
r; ~
of 110 to 450 and 90 to 5 par-ts by weight of at least one diene rubber.
The invention will be described in detail below.
The avera~e chaîn length of 1,4-sequence defined in the invention is measured as follows. That is, the polybutadiene accordin~ to the invention is completely hyclrogena~ed with p-toluenesulfonyl hydrazide according to a method disclosed in Makromol. Chem., 163, l (1973) to obtain a hydrogenation product to be tested. In this case, the completion of hydrogenation is confirmed by means of Hl-NM~. Then, the hydrogena~ion product or hydrogenated polybutadiene is measured with respect to average chain length of 1,4-sequence under the :Eollowing conditions using a nuclear magnetic resonance (NMR) apparatus of F~-lO0 Model made by Nippon Denki Kabushiki Kaisha:
Concentration of test sample : 300 mg/2 ml 1,2,4-trichlorobenzene with perdeuterobenzene, use of lO mm~ probe for l~C-NMR, Carrier frequency : 25.05 MHz, internal lock system, Flip angle : 45, Pulse width : 6 ~sec, Ac~uisition time : 5.0 sec, Spectrum sweep width : 2 KHz, Measuring tempera~ure : 125C, Internal reference : HMDS, Number of scan : llOxlO0 to l90xlO0 times.
~ 33~
Fu:rther, a-verage chain lengLhs of 1,2-sequence and 1,4-sequence are analyzed by the following equa-tions according to a method disclosed in J. Polymer Sci., Polymer Physics Edition, 13, 1975 (1975):
Average chain length of 1~2-sequence = 5I + 6 8 Average chain length of 1,4-sequence = ~ 8I 104I 11 , wherein each of I5, 1~, I8, Ig~ Ilo and I11 is an intensity o peak area at each of 37.2, 34.8, 34.0, 31.0~ 30.5 and 30.0 ppm. The assignment of the analytical results is shown in the following Table 1.
~ ~, ~3~
Table l Chemical Equation ~Ll Assignment shi-F-t (ppm) L2 r Il k r~2 (r~l)N01(13rl~ /V\(\~ V\/V 40-4 I2 = kNolo /V\/yVVVV 40 . 3 ~3 2k ?r~l NOl(l)rlO /V\~ (VVV 39 7 = kNollo /VV\~VVV\ 39.O
Is = 2k ~0 NOl(l)rl /V~yy\/v 37.2 r~O Ol ( l ) rlO /Vyyyv\ 34 . 8 r I7 21c ~O Nol(l)rl /\/~y\~/\ 34 5 I8 = 21cNolo /V\~/\ 34. O
19 = kNlo1 /yVVy\ 31. O
10 ~_o l O ( O ) sOl y\~v\~Vy\ 30 . 5 Ill k ~0 (4s~3 )Nlo ( o ~ sO] yv'~/vyv I12 = 2kNolo /V\~y\~v 27 . 3 I15 = kNolo /VvyVv 26. 7 Il6 = kNolo VVV\~VV ll.1 V~
~3 Ir ~
Note) I1, I2, ..., I16 shows an intensity of peak area at respective chemical shift, and r is 1,2-sequence, and s is 1,4-sequence.
~2 : found value of chemical shift.
Further J a heat vf fusion of the hydrogenation product of polybu-tadiene according to the invention is equivalent to the average chain length of 1,4-sequence, but it is preferable within a range of 42-135 cal/g.
The heat of fusion is measured from a fusion peak area obtained by placing abouL 10 mg of the hydrogenated poly-butadiene on an alwminum dish and raising temperature at a rate of 20C/min in a differential scanning calorimeter ~made by Rigaku Corp.). When the heat of fusion is less than 42 cal/g, the average chain length of 1,4-sequence does not rea$h into 110, while when the heat of fus:ion exceeds 135 cal/g, the average chain length of 1,4-sequence also exceeds 450.
The content of cis-1,4 bond is measured by means of the NMR apparatus.
The polybutadiene according to the invention having a particular average chain length of l,4-sequence can be produced, for example, by polymerizing butadiene in the presence of a catalyst consisting of a combination of a compound of lan~hanum series rare ear-th element (herein-after referred to as Ln compound), an organoaluminum compound and Lewis acid a-nd/or Lewis base.
As the Ln compound, there are used halides, carboxylates, alcoholates 9 thioalcvholates, amides and -the 37i~
like of metals having an atomic number of 57-71.
As the organoaluminum compound, ~here are used ones having a general formula of AlRlR2R3, wherein Rl, R2 and R3 are the same or differen~ and represent a hydrogen atom or a hydrocarbon residue havillg a carbon atom of 1-8, respectively.
As the Lewis acid, there are used aluminum halides having a general formula of AlXnR3 n~ wherein X is a halogen atom, R is a hydrocarbon residue and n is 1, 1.5, 2 or 3, or the other metal halides.
The Lewis base is used for solubilizing the Ln compound in an organic solvent. For instance, acetylacetone, ketone and the like are preferably used.
The mole ratio of butadiene to Ln compound is 5x10~-5x106, preferably 103-105. The mole ratio of AlR1R2R3 to Ln compound is 5-500, preferably 10-300. The mole ratio of halide in Lewis acid to Ln compound is 1-10, preferably 1~5-S. The mole ratio of I.ewis base to Ln compound is noL less than O.S, preferably 1-20.
According to the invention, the average chain length o~ 1,4-sequence is 110-450, preferably 130-300.
When the average chain length is less than 110, there is no effect for the improvement of cut growth resistance, while when the average chain length exceeds 450, the resulting polybutadiene is apt to be fatigued. For instance, when the polybu~adiene is subjected to repetitive stretching in a given direction over a long ~ime, a tear s~rength after a cut is formed in parallel with the stretching direction considerably reduces.
The polybutadiene according to the inventio-n has a content of cis-1,4 bond of a~ leas-t 70%, preferably no~
less ~han 90/O~ more particwlar:Ly 90-98%. When the content o-f cis-1,4 bond is less than 70%, the property of low energy loss disappears.
As the diene rubber to 'he used in the inven~ion, mention may be made of natural rubber, polyisoprene rubber, styrene~'butadiene copolymer rub'ber, acrylonitrile-butadiene copolymer rubber, ethylene-propylene-diene terpolymer rubber, isobutylene-isoprene copolymer rubber, halogenated-(isobutylene-isoprene copolymer) rubber and the like.
In the rubber composition according to the invention, the blending ratio of polybutadiene to diene ru'bber is 10-95 parts by weight to 90-5 parts by weight, preferably 30-95 parts by ~eight to 70-5 par~s by weight.
When the amount of polybutadiene rubber is less than 10 parts by weight, the blencling effect is not obtained, while when the amount of polybutadiene exceeds 95 parts by weight, the roll workabi:Lity becomes impractically poor.
To 100 parts by weight of the rubber composition according to the invention may be added 20-120 parts by weight of an inorganic filler and 0 5-10 parts by weight of a vulcanizing agent to form a curable rubber composition.
As the inorganic filler, use may be made of silicic anhydride, calcium carbonate, magnesium carbonate, talc, iron sulfide, iron oxide, bentonite, zinc white~
diatomaceous earth, china cla~, clay, alumina, titanium oxide, carbon black and the like When the amount of inorganic filler i5 less than 20 parts by weight, sufficient rein~orcing effec-t is not o'btained, while when -the amount of inorgan:ic filler exceeds 120 parts by weight, the ~33~'~
workability considerably lowers.
As the vulcaniæ:ing agent, mention ma.y be made of sulfur, p-quinonedioxime, p,p'-dibenzoylquinonedioxime, 4,4'-dithiodimorpholine, poly-p-dinitrobenzene5 ammoni.um benzoate, alkylphenol dis-ulficle and the like. Further, such a vulcanizing agent may be used together with peroxide.
~hen the amount of vulcanizing agent is ]ess than 0.5 part by weight, sufficient vulcanizing ef:Eect cannot be expected, while when the amount of vulcanizing agent exceeds 10 par-ts by wei.ght, ~.he resulting vulcani.zate is too hard and the elasticity of rubber in itself cannot be expected.
To the ruhber composition according to the invention may be added additives usually used in rubber industry such as softener, process oil, pigment, vulcaniza-lS tion accelerator and the lilce in addîtion to the above mentioned additives. Carbon black is preferable to have an iodine adsorption number of 30-150 mg/g and a dibutyl phthalate adsorption number of 45-140 cm3/100 g.
The mixing of i.ngredients forming the rubber composition according to the invention is per.Eormed by means of roll mill, Banbury mixer, extruder or the like in the usual manner. In this case, it is favorable to uniformly mix these ingredients at a state near the orcler of molecule.
The rubber compositions accord.ing to the invention are excellent in the fracture properties and cut growth resistance, so that they can wi.dely be used as industrial goods such as tires, conveyor belts, hoses and the like.
The following examples are given in illustration o-f the invention and are not intendecl as limitations thereof.
g 7'.~
Examples 1-4 Into a sufficiently dried glass autoclave of 5 Q
capacity was charged 2.5 kg of cyclohexane under a nitrogen atmosphere and further 0. 5 kg of butadiene, and then the temperature of the autoclave was raised to 60C. A reaction product of 138.9 mM of triethylaluminum, 2.31 mM of diethyl-aluminum bromide, 0.926 mM of neodymium octenoate and 1.85 mM of acetylacetone was previously aged as a catalyst in another vessel in the presence of 0.1 g of butadiene and then charged into the autoclave a~ once to star~
polymerization. After two hours of polymerization, -the degree of conversion reached to 100%. At this time, 5 ml of methanol solution containi.ng 2,6-di-tert-butyl cresol as an antioxidant was pourecl into the autoclave to stop polymerization reaction. The resulting polymerization product was subjected to st.eam stripping in the usual manner and dried on a hot roll ot 110C to obtain a poly-butadi.ene, which is called as Sample No. 4 hereinafter.
Ln the following Table 2 are shown measured values of average chain length of 1,4-sequence, micro-structure and calorimetric analysis of various polybutadiene samples.
In Table 2, Sample No. 1 is a polybutadiene rubber made by Anic Corp. using an uranium catalyst.
Sample No. 2 is obtained by dissolving each of Sample Nos. 1 and 4 in n-hexane and blending them at a blending ratio of Sample No. 1 to Sample No. 4 of 1:4. Sample No. 3 is obLained by blending Sample No. 1 and Sample No. 4 at a blending ratio of 4:6 in the same manner as described on Sample No. 2. Sample No. 6 is a polybutadiene rubber 37'~
made by Japan Synthetic Rubber Kabushiki Kaisha (trade mark ~R01). Sample No. 5 is obtained by dissolving each of Sample Nos. 4 and 6 in n-hexane and blending ~hem at a blending ratio of Sample No. 4 to Sample No. 6 of 1:4. Sample No, 7 is a polybu-~adiene rubber made by Ube Kosan Kabushiki Kaisha (trade mark UBEPOL 150). Sample No. 8 is a polybutadiene rubber made by Japan Synthetic Rubber Kabushiki Kaisha (trade mark BR02). Sample No. 9 is a polybutadiene rubber made by Philips Chemical Company (trade mark CIS-4 1203)... Sample No. 10 is a polybutadiene rubber made by Asahi Kasei Kabushiki Kaisha (trade mark DIENE 35 NF).
Table 2 ].5 \ A~erage chain Microstructure Calorimetric \ Items lengths of analysis \ 1,4- and 1,2-Poly- \ sequences cis;1,4 tla45 1j2 fusatOnf Tm butadiene \ 1,4 1,2 (%) (cal/g) Sample No. 1 523 1.0 97.4 1.2 1.4156 130 Sample No. 2 441 1.0 97.0 1.5 1.5130 129 Sample No. 3 300 1.0 96.2 2.0 1.895 129 Sample No~ 4 152 1.0 95.3 2.5 2.251 129 Samp].e No. 5 113 1.0 95.0 2.8 2.2 43 124 Sample No. 6 10~ 1.0 94.9 2.9 2.243 123 Sample No. 7 70 1.0 9~5 2.6 2.939 120 Sample No. 8 20 1.0 94.2 2.5 3.332 112 Sample No. 9 18 1.0 88.8 4.7 5.229 1~0 Sample No. 10 14 1.1 32.7 53.2 14.024 93 0 Note) Heat o fusion (cal/g) was measured from the hydro~enated sample as previously mentioned.
3'7~
Then, each pclybutad:iene of Sample Nos. 1-10 was used to form a rubber composit:ion according to the follow-ing compounding recipe:
Compounding recipe (part by weight):
polybutadiene 70 natural rubber 30 carbon black HAF 45 aromatie oil 5 stearie aeid . 2.0 antioxidant (SANTOFLEX B ) 1.O
zinc white 3.0 vulcanization aecelerator (NQBS) 1.0 sulfur 1.5 Then, the resulting rubber eomposi.tion was eured under a euring eonclitîon of 140Cx40 min and its cured properties were measured to obtain results as shown in the following Table 3.
* Trade Mark Table 3 S 1 Tensile ReSilience Flex Cut growth Tear No. strength ~R.T.) resistance resistance strength Comparative No. 1 241 67 98 254 71 example Example 1 No. 2 237 68 154 207 104 E~ample 2 No. 3 239 69 176 256 103 Example 3 No. 4 238 70 188 29g 105 Example 4 No. 5 235 68 111 289 101 r Comparative No. 6 203 65 100 100 100 ~xample 2 Comparative No. 7 201 65 100 98 10 example 3 Comparative No. 8 189 63 9g 84 108 example 4 Comparative No. 9 199 67 95 102 105 example 5 Comparative No. 10 178 62 86 85 93 example 6 ~33~
~1) The tensile strength was measured according to a method of JIS K6301.
(2) The resilience was measured by means of a Dunlop tripsometer according to a method of B.S. 903 (1950).
(3) The flex resistance was measured according to a flex fatigue -test of JIS K6301. In this case, a time till crack occurred in a tes-t piece having no cut is expressed by an index on a basis that Comparative Example 2 is 100.
I'ime till occurrence of crack . = in each test piece x 00 lex reslstance Time till occurrence of crack in Comparative Example 2 (4~ The cut growth resistance was measured by forming a cut of 0.3 mm length in a center of a test piece having a size of 60 mmxlOO mmxlO ~n and giving a stretching strain to ~he test piece under conclitions of vibration number of 300 cycles/min and strain of 50%. In this case, a time till cut grows to 20 mm is expressed by an index on a ba~is that Comparative Example 2 is lOO.
Time till cut growth of 20 mm in each test piece ~
Cut growth ~esistance = Time till cut growth of x luv 20 mm i~ Compa~ative Example 2 (5) The tear strength was measured in order to examine orientation fatigue property. After a test piece having a size of 150 mmxl50 mmx2 mm was subjected to repetitive stretching of 200,000 times under conditiolls of 300 cycles/min and 50% strain, a sample of JIS No. 3 Dumb-bell shaped type was punched out from the tes~ piece 3'7~
in a direction opposite to the stretching direction and a cu~ of 0.3 mm length was forllled on the sample in the stretching direc-tion. Then, the strength at rupture was measured by stre-tching the sample at a ra-te of 500 mm/min.
Similarly, the strength at nlpture was .measured with respect to the test piece having no hysteresis.
Strength at rupture after fatigue x 100 Tear strength Strength at rupture before fatigue Examples 5-9 The properties of cured rubber compositions were measured by changing the kincl and amoun-t of diene :rubber, inorganic filler and vulcanizing agent to obtain results as shown in the following Table 4.
337~
Table 4 Example Example Example Example Example Polybutadiene 50 50 50 30 30 Natural rubber 50 50 50 50 50 Carbon blaclc ISAF 1) 20 45 75 - -Car~on black CPF 2) - - - 40 40 Silicic anhydride 3) 2 10 10 Clay 4) - ~ 30 - -Aromatic oil 5 5 5 SANTOFLÆX B~ 1 1 1 1 1 Stearic acid 2 2 2 2 2 Zinc white 3 3 3 3 3 Vulcaniza~ion 0 8 l 4 0 accelerator NOBS0.8 . 0.8 .. ,9 Sulf~l~ 1.5 1.5 1.5 ~.3 1.5 Alkylphenol _ _ _ 0,3 1.5 Total amoun-t of inorganic fillers22 55 115 40 40 1)+2)~3)-~4) Total amount of vulcanizing agents1.5 1.5 1.5 0.6 3.0 Tensile stren~kt/ 2 ) 211 248 236 218 241 Cut growth 182 285 145 148 150 resistance Flex resistance 128 183 120 120 132 Silicic anhydride : made by Nippon Silica Ko~yo Kabushiki Kaisha, NIPSIL VN~3 (trade mark) Clay : a].uminum silicate, made by Shiraishi Calciwn Kabushlki Kaisha, HA~D TOP
CLAY (trade mark) * Trade Mar~ - 16 -.~
Then, each pclybutad:iene of Sample Nos. 1-10 was used to form a rubber composit:ion according to the follow-ing compounding recipe:
Compounding recipe (part by weight):
polybutadiene 70 natural rubber 30 carbon black HAF 45 aromatie oil 5 stearie aeid . 2.0 antioxidant (SANTOFLEX B ) 1.O
zinc white 3.0 vulcanization aecelerator (NQBS) 1.0 sulfur 1.5 Then, the resulting rubber eomposi.tion was eured under a euring eonclitîon of 140Cx40 min and its cured properties were measured to obtain results as shown in the following Table 3.
* Trade Mark Table 3 S 1 Tensile ReSilience Flex Cut growth Tear No. strength ~R.T.) resistance resistance strength Comparative No. 1 241 67 98 254 71 example Example 1 No. 2 237 68 154 207 104 E~ample 2 No. 3 239 69 176 256 103 Example 3 No. 4 238 70 188 29g 105 Example 4 No. 5 235 68 111 289 101 r Comparative No. 6 203 65 100 100 100 ~xample 2 Comparative No. 7 201 65 100 98 10 example 3 Comparative No. 8 189 63 9g 84 108 example 4 Comparative No. 9 199 67 95 102 105 example 5 Comparative No. 10 178 62 86 85 93 example 6 ~33~
~1) The tensile strength was measured according to a method of JIS K6301.
(2) The resilience was measured by means of a Dunlop tripsometer according to a method of B.S. 903 (1950).
(3) The flex resistance was measured according to a flex fatigue -test of JIS K6301. In this case, a time till crack occurred in a tes-t piece having no cut is expressed by an index on a basis that Comparative Example 2 is 100.
I'ime till occurrence of crack . = in each test piece x 00 lex reslstance Time till occurrence of crack in Comparative Example 2 (4~ The cut growth resistance was measured by forming a cut of 0.3 mm length in a center of a test piece having a size of 60 mmxlOO mmxlO ~n and giving a stretching strain to ~he test piece under conclitions of vibration number of 300 cycles/min and strain of 50%. In this case, a time till cut grows to 20 mm is expressed by an index on a ba~is that Comparative Example 2 is lOO.
Time till cut growth of 20 mm in each test piece ~
Cut growth ~esistance = Time till cut growth of x luv 20 mm i~ Compa~ative Example 2 (5) The tear strength was measured in order to examine orientation fatigue property. After a test piece having a size of 150 mmxl50 mmx2 mm was subjected to repetitive stretching of 200,000 times under conditiolls of 300 cycles/min and 50% strain, a sample of JIS No. 3 Dumb-bell shaped type was punched out from the tes~ piece 3'7~
in a direction opposite to the stretching direction and a cu~ of 0.3 mm length was forllled on the sample in the stretching direc-tion. Then, the strength at rupture was measured by stre-tching the sample at a ra-te of 500 mm/min.
Similarly, the strength at nlpture was .measured with respect to the test piece having no hysteresis.
Strength at rupture after fatigue x 100 Tear strength Strength at rupture before fatigue Examples 5-9 The properties of cured rubber compositions were measured by changing the kincl and amoun-t of diene :rubber, inorganic filler and vulcanizing agent to obtain results as shown in the following Table 4.
337~
Table 4 Example Example Example Example Example Polybutadiene 50 50 50 30 30 Natural rubber 50 50 50 50 50 Carbon blaclc ISAF 1) 20 45 75 - -Car~on black CPF 2) - - - 40 40 Silicic anhydride 3) 2 10 10 Clay 4) - ~ 30 - -Aromatic oil 5 5 5 SANTOFLÆX B~ 1 1 1 1 1 Stearic acid 2 2 2 2 2 Zinc white 3 3 3 3 3 Vulcaniza~ion 0 8 l 4 0 accelerator NOBS0.8 . 0.8 .. ,9 Sulf~l~ 1.5 1.5 1.5 ~.3 1.5 Alkylphenol _ _ _ 0,3 1.5 Total amoun-t of inorganic fillers22 55 115 40 40 1)+2)~3)-~4) Total amount of vulcanizing agents1.5 1.5 1.5 0.6 3.0 Tensile stren~kt/ 2 ) 211 248 236 218 241 Cut growth 182 285 145 148 150 resistance Flex resistance 128 183 120 120 132 Silicic anhydride : made by Nippon Silica Ko~yo Kabushiki Kaisha, NIPSIL VN~3 (trade mark) Clay : a].uminum silicate, made by Shiraishi Calciwn Kabushlki Kaisha, HA~D TOP
CLAY (trade mark) * Trade Mar~ - 16 -.~
Claims (10)
1. A rubber composition having excellent fracture properties and cut growth resistance, consisting of 10 to 95 parts by weight of polybutadiene having a content of cis-1,4 bond of at least 70% and an average chain length of 1,4-sequence of 110-450 and 90 to 5 parts by weight of at least one diene rubber.
2 A rubber composition according to claim 1, wherein said average chain length of 1,4-sequence of polybutadiene is 130 to 300.
3. A rubber composition according to claim 1, wherein said content of cis-1,4 bond of polybutadiene is at least 90%, preferably 90-98%.
4. A rubber composition according to claim 1, wherein a heat of fusion of hydrogenation product of said polybutadiene is 42 to 135 cal/g.
5. A rubber composition according to claim 1, wherein said diene rubber is selected from natural rubber, polyisoprene rubber, styrene-butadiene copolymer rubber, acrylonitrile-butadiene copolymer rubber, ethylene-propylene-diene terpolymer rubber, isobutylene-isoprene copolymer rubber and halogenated-(isobutylene-isoprene copolymer) rubber.
6. A rubber composition according to claim 1, wherein an amount of said polybutadiene is 30 to 95 parts by weight and an amount of said diene rubber is 70 to 5 parts by weight.
7. A curable rubber composition having excellent fracture properties and cut growth resistance, comprising adding 20 to 120 parts by weight of at least one inorganic filler and 0.5 to 10 parts by weight of a vulcanizing agent to 100 parts by weight of a rubber composition consisting of 10 to 95 parts by weight of polybutadiene having a content of cis-1,4 bond of at least 70% and an average chain length of 1,4-sequence of 110 to 450 and 90 to 5 parts by weight of at least one diene rubber.
8. A curable rubber composition according to claim 7, wherein said inorganic filler is selected from silicic anhydride, calcium carbonate, magnesium carbonate, talc, iron sulfide, iron oxide, bentonite, zinc white, diatomaceous earth, china clay, clay, alumina, titanium oxide and carbon black.
9. A curable rubber composition according to claim 8, wherein said carbon black has an iodine adsorption number of 30 to 150 mg/g and a dibutyl phthalate adsorption number of 45 to 140 cm3/100 g.
10. A curable rubber composition according to claim 7, wherein said vulcanizing agent is selected from sulfur, p-quinonedioxime, p,p'-dibenzoylquinonedioxime, 4,4'-dithio-dimorpholine, poly-p-dinitrobenzene, ammonium benzoate and alkylphenol disulfide.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56119303A JPS5821434A (en) | 1981-07-31 | 1981-07-31 | Polybutadiene rubber composition |
JP119,303/81 | 1981-07-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1193374A true CA1193374A (en) | 1985-09-10 |
Family
ID=14758076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000408228A Expired CA1193374A (en) | 1981-07-31 | 1982-07-28 | Polybutadiene rubber compositions |
Country Status (6)
Country | Link |
---|---|
US (1) | US4468496A (en) |
JP (1) | JPS5821434A (en) |
AU (1) | AU537966B2 (en) |
CA (1) | CA1193374A (en) |
DE (1) | DE3228547C2 (en) |
GB (1) | GB2102437B (en) |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60106470A (en) * | 1983-11-14 | 1985-06-11 | 住友ゴム工業株式会社 | Non-pressure tennis ball |
JPS60106471A (en) * | 1983-11-15 | 1985-06-11 | 住友ゴム工業株式会社 | Core for tennis ball |
JPH0781032B2 (en) * | 1985-08-29 | 1995-08-30 | 日本合成ゴム株式会社 | Rubber composition and method for producing the same |
JPS6354455A (en) * | 1986-08-23 | 1988-03-08 | Kurashiki Kako Kk | Temperature-sensitive rubber composition |
JPH0627219B2 (en) * | 1986-09-08 | 1994-04-13 | 日本合成ゴム株式会社 | Polybutadiene rubber composition |
JPH0774291B2 (en) * | 1987-05-29 | 1995-08-09 | 日本合成ゴム株式会社 | Anti-vibration rubber composition |
US5162409B1 (en) * | 1991-08-02 | 1997-08-26 | Pirelli Armstrong Tire Corp | Tire tread rubber composition |
US5558325A (en) * | 1993-08-05 | 1996-09-24 | Gencorp Inc. | Play balls or pressureless tennis balls |
US5622557A (en) * | 1995-05-22 | 1997-04-22 | Cabot Corporation | Mineral binders colored with silicon-containing carbon black |
US5830930A (en) * | 1995-05-22 | 1998-11-03 | Cabot Corporation | Elastomeric compounds incorporating silicon-treated carbon blacks |
US6323273B1 (en) | 1995-05-22 | 2001-11-27 | Cabot Corporation | Elastomeric compounds incorporating silicon-treated carbon blacks |
US6028137A (en) * | 1995-05-22 | 2000-02-22 | Cabot Corporation | Elastomeric compounds incorporating silicon-treated carbon blacks |
US6008272A (en) * | 1995-05-22 | 1999-12-28 | Cabot Corporation | Elastomeric compounds incorporating silicon-treated carbon blacks |
US5877238A (en) * | 1995-05-22 | 1999-03-02 | Cabot Corporation | Elastomeric compounds incorporating silicon-treated carbon blacks and coupling agents |
CA2221573C (en) * | 1995-05-22 | 2002-10-08 | Cabot Corporation | Elastomeric compounds incorporating partially coated carbon blacks |
US5798416A (en) * | 1995-07-18 | 1998-08-25 | Toyo Tire & Rubber Co., Ltd. | Automobile vibration-isolating rubber composition and automobile vibration-isolating device |
US5948835A (en) * | 1995-09-15 | 1999-09-07 | Cabot Corporation | Silicon-treated carbon black/elastomer formulations and applications |
EP0909212B1 (en) | 1996-06-14 | 2012-02-01 | Cabot Corporation | Use and method for use of modified carbon adsorbents |
US5747562A (en) | 1996-06-14 | 1998-05-05 | Cabot Corporation | Ink and coating compositions containing silicon-treated carbon black |
US5919855A (en) * | 1997-02-11 | 1999-07-06 | Cabot Corporation | Use of modified carbon black in gas-phase polymerizations |
US5885389A (en) * | 1997-03-06 | 1999-03-23 | The Goodyear Tire & Rubber Company | Tire with chafer composition |
DE10062860A1 (en) * | 2000-12-16 | 2002-06-27 | Henkel Teroson Gmbh | Rubber compositions with plastisol-like flow behavior |
KR100406518B1 (en) * | 2001-06-01 | 2003-11-20 | 한국타이어 주식회사 | Rubber composition for tire |
US8088868B2 (en) * | 2006-12-19 | 2012-01-03 | Bridgestone Corporation | Polymers functionalized with protected oxime compounds |
US8841376B2 (en) * | 2006-12-31 | 2014-09-23 | Bridgestone Corporation | Methods for identifying and utilizing rubber compositions with good wet traction performance |
US7765720B2 (en) | 2007-01-12 | 2010-08-03 | Nike, Inc, | Outsole for an article of footwear |
US7939175B2 (en) * | 2007-04-25 | 2011-05-10 | Veyance Technologies, Inc. | Non-halogenated rubber compounds for use in conveyor belts |
US8007917B2 (en) * | 2007-04-25 | 2011-08-30 | Veyance Technologies, Inc. | Non-halogenated rubber compounds for use in conveyor belts |
KR101657603B1 (en) | 2007-12-28 | 2016-09-19 | 가부시키가이샤 브리지스톤 | Hydroxyaryl functionalized polymers |
WO2009132514A1 (en) | 2008-04-29 | 2009-11-05 | 中国科学院长春应用化学研究所 | Isoprene or butadiene cis 1,4-polymeric bi-component catalyst system and polymerization process |
DE102008053888A1 (en) * | 2008-10-30 | 2010-05-06 | Lanxess Deutschland Gmbh | New process for the production of polybutadiene-containing moldings |
US20120258829A1 (en) * | 2011-04-07 | 2012-10-11 | Carlisle Intangible Company | Polybutadiene-based power transmission belting |
CN111386307B (en) * | 2017-11-24 | 2021-03-16 | Nok株式会社 | NBR composition for rubber laminate metal |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3060989A (en) * | 1959-08-17 | 1962-10-30 | Phillips Petroleum Co | Blends of cis-polybutadiene with either natural rubber or cis-polyisoprene, method of preparing same, and tire tread comprising same |
US3225122A (en) * | 1962-10-12 | 1965-12-21 | Phillips Petroleum Co | Prevention of cold flow in cis-polybutadiene by adding hydrogenated diene polymer |
-
1981
- 1981-07-31 JP JP56119303A patent/JPS5821434A/en active Granted
-
1982
- 1982-07-26 AU AU86401/82A patent/AU537966B2/en not_active Expired
- 1982-07-26 US US06/401,509 patent/US4468496A/en not_active Expired - Lifetime
- 1982-07-28 CA CA000408228A patent/CA1193374A/en not_active Expired
- 1982-07-30 DE DE3228547A patent/DE3228547C2/en not_active Expired
- 1982-08-02 GB GB08222246A patent/GB2102437B/en not_active Expired
Also Published As
Publication number | Publication date |
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AU537966B2 (en) | 1984-07-19 |
GB2102437B (en) | 1985-02-20 |
US4468496A (en) | 1984-08-28 |
GB2102437A (en) | 1983-02-02 |
JPH0125332B2 (en) | 1989-05-17 |
AU8640182A (en) | 1983-02-03 |
DE3228547A1 (en) | 1983-03-03 |
JPS5821434A (en) | 1983-02-08 |
DE3228547C2 (en) | 1985-09-19 |
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